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Anti-Inflammatory Effect of Supercritical-Carbon Dioxide Fluid Extract from Flowers and Buds of Chrysanthemum indicum Linnén

机译:菊花花和芽中超临界二氧化碳流体提取物的抗炎作用

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摘要

The aim of this study was to analyze the chemical composition and investigate the anti-inflammatory property of the supercritical-carbon dioxide extract from flowers and buds of C. indicum (CISCFE). The anti-inflammatory effect was evaluated in four animal models including xylene-induced mouse ear edema, acetic acid-induced mouse vascular permeability, carrageenan-induced mouse hind paw edema, and cotton pellet-induced rat granuloma formation. The results indicated that CISCFE significantly attenuated xylene-induced ear edema, decreased acetic acid-induced capillary permeability, reduced carrageenan-induced paw, and inhibited the cotton pellet-induced granuloma formation in a dose-dependent manner. Histopathologically, CISCFE abated inflammatory response of the edema paw. Preliminary mechanistic studies demonstrated that CISCFE decreased the MDA level via increasing the activities of anti-oxidant enzymes (SOD, GPx, and GRd), attenuated the productions of NF-κB, TNF-α, IL-1β, IL-6, PGE2 and NO, and suppressed the activities of iNOS and COX-2. In phytochemical study, 35 compounds were identified by GC-MS, and 5 compounds (chlorogenic acid, luteolin-7-glucoside, linarin, luteolin and acacetin) were reconfirmed and quantitatively determined by HPLC-PAD. This paper firstly analyzed the chemical composition by combining GC-MS with HPLC-PAD and explored possible mechanisms for the anti-inflammatory effect of CISCFE.
机译:这项研究的目的是分析化学成分,并研究印度菊(C.indicum)的花和芽(CISCFE)中超临界二氧化碳提取物的抗炎特性。在四种动物模型中评估了抗炎作用,其中包括二甲苯诱导的小鼠耳部水肿,乙酸诱导的小鼠血管通透性,角叉菜胶诱导的小鼠后爪水肿和棉丸诱导的大鼠肉芽肿形成。结果表明,CISCFE显着减轻了二甲苯引起的耳部水肿,降低了乙酸引起的毛细血管通透性,减少了角叉菜胶引起的爪子,并以剂量​​依赖的方式抑制了棉丸引起的肉芽肿的形成。在组织病理学上,CISCFE减轻了水肿爪的炎症反应。初步的机理研究表明,CISCFE通过增加抗氧化酶(SOD,GPx和GRd)的活性降低了MDA含量,减弱了NF-κB,TNF-α,IL-1β,IL-6,PGE2和否,并抑制了iNOS和COX-2的活性。在植物化学研究中,通过GC-MS鉴定了35种化合物,并通过HPLC-PAD对5种化合物(绿原酸,木犀草素7-葡糖苷,柠檬苦素,木犀草素和阿沙西汀)进行了重新确认和定量测定。本文首先结合GC-MS和HPLC-PAD分析了化学成分,并探讨了CISCFE抗炎作用的可能机制。

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